Dompe US, Inc.

FDA Device Registration & Listing · San Mateo, CA, US · Registration 3017521274

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3017521274
FEI Number
3017521274
Entity Name
Dompe US, Inc.
City/State/Country
San Mateo, CA, US
Establishment Address
400 S El Camino Real Ste 400, San Mateo, CA 94402, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Dompe farmaceutici S.p.A. (Owner Number: 10057047)
Owner / Operator Contact Address
Via Campo di Pile, L’Aquila, IT-65 67100, IT
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Pipette SI5 Sterile Dropper SI6

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2018-05-11

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dompe farmaceutici S.p.A.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3004216297 DOMPE FARMACEUTICI S.P.A. L Aquila Abruzzo, IT

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017521274. Last updated year: 2026. Please use registration number 3017521274 when referencing this establishment in official correspondence.
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